新生隐球菌
隐球菌
效力
化学
微生物学
抗真菌
体内
细胞毒性
酵母
广谱
体外
生物
组合化学
生物化学
生物技术
作者
Nereu Junio Cândido Oliveira,Valtair Severino dos Santos,Isabella Campolina Pierotte,Victor Augusto Teixeira Leocádio,Luiz Felipe de Andrade Santana,Gabriel Marques,Ícaro F. Protti,Saulo Fehelberg Pinto Braga,Markus Kohlhoff,Túlio Resende Freitas,Adriano de Paula Sabino,Thales Kronenberger,José Eduardo Gonçalves,Susana Johann,Daniel Assis Santos,Isabela Costa César,Vinícius Gonçalves Maltarollo,Renata Barbosa de Oliveira
标识
DOI:10.1021/acs.jmedchem.3c01105
摘要
Opportunistic fungal infections represent a global health problem, mainly for immunocompromised individuals. New therapeutical options are needed since several fungal strains show resistance to clinically available antifungal agents. 2-Thiazolylhydrazones are well-known as potent compounds against Candida and Cryptococcus species. A scaffold-focused drug design using machine-learning models was established to optimize the 2-thiazolylhydrazone skeleton and obtain novel compounds with higher potency, better solubility in water, and enhanced absorption. Twenty-nine novel compounds were obtained and most showed low micromolar MIC values against different species of Candida and Cryptococcus spp., including Candida auris, an emerging multidrug-resistant yeast. Among the synthesized compounds, 2-thiazolylhydrazone 28 (MIC value ranging from 0.8 to 52.17 μM) was selected for further studies: cytotoxicity evaluation, permeability study in Caco-2 cell model, and in vivo efficacy against Cryptococcus neoformans in an invertebrate infection model. All results obtained indicate the great potential of 28 as a novel antifungal agent.
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